Details
Stereochemistry | ABSOLUTE |
Molecular Formula | C21H20O12 |
Molecular Weight | 464.3763 |
Optical Activity | UNSPECIFIED |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
OC[C@H]1O[C@@H](OC2=CC(O)=C3C(=O)C(O)=C(OC3=C2)C4=CC=C(O)C(O)=C4)[C@H](O)[C@@H](O)[C@@H]1O
InChI
InChIKey=BBFYUPYFXSSMNV-HMGRVEAOSA-N
InChI=1S/C21H20O12/c22-6-13-15(26)17(28)19(30)21(33-13)31-8-4-11(25)14-12(5-8)32-20(18(29)16(14)27)7-1-2-9(23)10(24)3-7/h1-5,13,15,17,19,21-26,28-30H,6H2/t13-,15-,17+,19-,21-/m1/s1
Molecular Formula | C21H20O12 |
Molecular Weight | 464.3763 |
Charge | 0 |
Count |
|
Stereochemistry | ABSOLUTE |
Additional Stereochemistry | No |
Defined Stereocenters | 5 / 5 |
E/Z Centers | 0 |
Optical Activity | UNSPECIFIED |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Proposed active constituents of Dipladenia martiana. | 2001 Dec |
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Chemical constituents from the leaves of Boehmeria rugulosa with antidiabetic and antimicrobial activities. | 2009 Dec |
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Antioxidant activities of new flavonoids from Cudrania tricuspidata root bark. | 2009 Feb |
|
Phenolic compounds in leaves of Alchornea triplinervia: anatomical localization, mutagenicity, and antibacterial activity. | 2010 Aug |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 10:09:34 GMT 2023
by
admin
on
Sat Dec 16 10:09:34 GMT 2023
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Record UNII |
177033M1DL
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Record Status |
Validated (UNII)
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Record Version |
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-
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5282160
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28529
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DTXSID30964161
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177033M1DL
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491-50-9
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m9421
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admin on Sat Dec 16 10:09:34 GMT 2023 , Edited by admin on Sat Dec 16 10:09:34 GMT 2023
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115917
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Related Record | Type | Details | ||
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SOLVATE->ANHYDROUS | |||
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SALT/SOLVATE -> PARENT | |||
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PARENT -> CONSTITUENT ALWAYS PRESENT |